Profile of Cerebrospinal microRNAs in Fibromyalgia

被引:79
作者
Bjersing, Jan L. [1 ]
Lundborg, Christopher [2 ]
Bokarewa, Maria I. [1 ]
Mannerkorpi, Kaisa [1 ,3 ]
机构
[1] Univ Gothenburg, Inst Med, Dept Rheumatol & Inflammat Res, Sahlgrenska Acad, Gothenburg, Sweden
[2] Univ Gothenburg, Inst Clin Sci, Dept Anaesthesiol & Intens Care Med, Sahlgrenska Acad, Gothenburg, Sweden
[3] Univ Gothenburg, Sahlgrenska Acad, Univ Gothenburg Ctr Person Centred Care GPCC, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
LONG-TERM; EXPRESSION; PAIN; GROWTH; PROTECTS; IMPACT; INFLAMMATION; RELIABILITY; INVOLVEMENT; EXERCISE;
D O I
10.1371/journal.pone.0078762
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Introduction: Fibromyalgia (FM) is characterized by chronic pain and reduced pain threshold. The pathophysiology involves disturbed neuroendocrine function, including impaired function of the growth hormone/insulin-like growth factor-1 axis. Recently, microRNAs have been shown to be important regulatory factors in a number of diseases. The aim of this study was to try to identify cerebrospinal microRNAs with expression specific for FM and to determine their correlation to pain and fatigue. Methods: The genome-wide profile of microRNAs in cerebrospinal fluid was assessed in ten women with FM and eight healthy controls using real-time quantitative PCR. Pain thresholds were examined by algometry. Levels of pain (FIQ pain) were rated on a 0-100 mm scale (fibromyalgia impact questionnaire, FIQ). Levels of fatigue (FIQ fatigue) were rated on a 0-100 mm scale using FIQ and by multidimensional fatigue inventory (MFI-20) general fatigue (MFIGF). Results: Expression levels of nine microRNAs were significantly lower in patients with FM patients compared to healthy controls. The microRNAs identified were miR-21-5p, miR-145-5p, miR-29a-3p, miR-99b-5p, miR-125b-5p, miR-23a-3p, 23b-3p, miR-195-5p, miR-223-3p. The identified microRNAs with significantly lower expression in FM were assessed with regard to pain and fatigue. miR-145-5p correlated positively with FIQ pain (r=0.709, p=0.022, n=10) and with FIQ fatigue (r=0.687, p=0.028, n=10). Conclusion: To our knowledge, this is the first study to show a disease-specific pattern of cerebrospinal microRNAs in FM. We have identified nine microRNAs in cerebrospinal fluid that differed between FM patients and healthy controls. One of the identified microRNAs, miR-145 was associated with the cardinal symptoms of FM, pain and fatigue.
引用
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页数:6
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